EP2801583A1 - Gentechnisch veränderte menschliche natürliche Killerzelllinien - Google Patents
Gentechnisch veränderte menschliche natürliche Killerzelllinien Download PDFInfo
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- EP2801583A1 EP2801583A1 EP20140171739 EP14171739A EP2801583A1 EP 2801583 A1 EP2801583 A1 EP 2801583A1 EP 20140171739 EP20140171739 EP 20140171739 EP 14171739 A EP14171739 A EP 14171739A EP 2801583 A1 EP2801583 A1 EP 2801583A1
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Definitions
- This invention relates generally to certain natural killer (NK) cell lines that have been genetically engineered to express a cell surface receptor protein that participates in antibody-dependent cellular cytotoxicity responses. More specifically, the present invention relates to a natural killer cell line NK-92 which, in a first embodiment, has been modified to express an Fc cell surface receptor protein such as CD16, and in a second embodiment, has been modified to express both an Fc cell surface receptor protein such as CD 16 and one or more of the associated accessory signaling proteins such as FcR- ⁇ or TCR- ⁇ and/or a cytokine such as IL-2.
- NK natural killer
- NK natural killer
- ADCC antibody-dependent cellular cytotoxicity
- NK cells are a class of lymphocytes that typically comprise approximately 10% of the lymphocytes in a human.
- the primary function of NK cells is to provide an innate cellular immune response against tumor and infected (target) cells. Roles in the priming and regulation of humoral immune response, fetal development and the elimination of stressed or damaged normal cells have also been demonstrated and/or are considered to be likely.
- NK cells which are characterized as having a CD3 - /CD56 + phenotype, display a variety of activating and inhibitory cell surface receptors.
- NK cell receptor The binding or ligation of an activating NK cell receptor to the corresponding ligand on a target cell triggers the NK cell to exert a cytotoxic effect directly against the target cell and to secrete a variety of cytokines that perform functions such as the stimulation and recruitment of other elements of the immune system to act against the target.
- Activated NK cells lyse target cells via the secretion of the enzymes perforin and granzyme, stimulation of apoptosis-initiating receptors and other less well characterized mechanisms.
- NK cell inhibitory receptors predominantly engage with major histocompatibility complex class I ("MHC-I") proteins on the surface of a normal cell. When so engaged, these inhibitory receptors prevent NK cells from becoming activated.
- MHC-I molecules define cells as "belonging" to a particular individual. As expression of these MHC-I molecules can prevent NK cell activation toward a target cell, it is thought that NK cells can be activated only by cells on which these "self" MHC-I molecules are missing or defective, such as is often the case for tumor or virus-infected cells.
- NK cell phenotype and activation pattern are distinct from that exhibited by cytotoxic T-lymphocytes ("CTLs," CD3 + /CD56 - /GD8 + phenotype) that are activated by target cells that display small foreign peptide fragments derived from viruses or tumor cells attached to the surface MHC-I molecules.
- CTLs cytotoxic T-lymphocytes
- NK cells evolved as a response to tumor and infected cells that evade destruction by CTLs through suppression or disruption of the display of peptide-presenting MHC-I molecules.
- NK cells have been evaluated as a therapeutic agent in the treatment of certain cancers.
- the NK cells used for this purpose are isolated from the peripheral blood lymphocyte ("PBL") fraction of blood from the subject, expanded in cell culture in order to obtain sufficient numbers of cells, and then re-infused into the subject.
- PBL peripheral blood lymphocyte
- preparation of the autologous NK cells is expensive, labor intensive and time consuming.
- quality control of these cells is complicated by each preparation being subject specific.
- the quantity of NK cells that can be isolated from a subject can vary substantially, and these cells are often deficient in proliferative ability and/or cytotoxic activity.
- NK cells are a therapeutic agent that results from the presence of surface antigens on the cells that can evoke an immune rejection response when the cells are infused into a subject other than the one from which they were isolated. This necessitates careful MHC-I cross-matching between the donor and the recipient as well as the need to immuno-suppress the recipient.
- NK-92 The NK-like cell line NK-92 was discovered in the blood of a subject suffering from a non-Hodgkins lymphoma. NK-92 cells lack the major inhibitory receptors that are displayed by normal NK cells, but retain the majority of the activating receptors. Characterization of the NK-92 cell line (Gong et al., 1994; Yan et al., 1998) revealed that NK-92 cells are cytotoxic to a significantly broader spectrum of tumor and infected cell types than are NK cells, and further that they often exhibit higher levels of cytotoxicity toward these targets. NK-92 cells do not, however, attack normal cells nor do they elicit an immune rejection response.
- NK-92 cells can be readily and stably grown and maintained in continuous cell culture and, thus, can be prepared in large quantities under c-GMP compliant quality control. This combination of characteristics has resulted in NK-92 being entered into presently on-going clinical trials for the treatment of multiple types of cancers.
- NK-92 cells retain almost all of the activating receptors and cytolytic pathways associated with NK cells, they do not express the CD16 receptor and, therefore, cannot lyse target cells via the ADCC mechanism. This means that despite their other benefits, NK-92 cells cannot potentiate the anti-tumor and anti-infection effects of endogenous or exogenous antibodies in the manner of NK cells.
- Other NK-like cell lines in addition to NK-92 are also known. Some of these other NK-like cell lines express CD16, but this expression is unstable; the cells are typically difficult to grow in cell culture; and few exhibit robust cytotoxic activity. For these reasons, only NK-92 of the currently known NK-like cell lines is a viable candidate as a therapeutic agent even though it lacks CD 16 and, consequently, the ability to kill target cells via the ADCC mechanism.
- NK cell lines have been found to be recalcitrant to gene transfer, a feature that has hampered the development of such cell lines for research or therapeutic purposes.
- transformation efficiencies of only 5-15% and 10-20% have been achieved using particle-mediated gene transfer or retroviral transduction (Nagashima et al., 1998; Tam et al., 1999).
- NK-92 cell lines that stably expresses the CD16 cell surface receptor are currently unavailable.
- the various embodiments of the invention provide or utilize an NK-92 cell modified to express a Fc receptor such as CD16 (Fc ⁇ RIII-A), or more generally, any other Fc receptor, on the surface of the cell.
- a Fc receptor such as CD16 (Fc ⁇ RIII-A), or more generally, any other Fc receptor, on the surface of the cell.
- the invention is directed to NK-92 cells modified to express a Fc receptor on a surface of the cell;
- the Fc receptor can be an activating Fc ⁇ receptor, CD16 (Fc ⁇ RIII-A), or any member of an Fc receptor class, such as FC ⁇ RI (CD64), FC ⁇ RII (CD32), FC ⁇ RIII, FcRn, Fc ⁇ and Fc ⁇ .
- the Fc receptors can be of any binding affinity for their ligands, or fragments of their ligands, including low- and high-binding affinity forms.
- the NK-92 cells can be modified by introducing a polynucleotide that encodes a polypeptide having at least 70%, 80%, 90%, 95%, 99% or 100% identity to the amino acid sequences of SEQ ID NO:1 or SEQ ID NO:2; one such polynucleotide includes SEQ ID NO:3.
- the NK-92 cells can be further modified to express one or more associated accessory signaling polypeptides, cytokines, or fragments thereof; such expression can correlate with increased surface expression of the Fc receptor.
- Associated accessory signaling polypeptides include Fc ⁇ RI- ⁇ (SEQ ID NO:5)or TCR- ⁇ (SEQ ID NO:7). Expression of a cytokine (such as interleukin-2) can also correlate with viability or cytotoxicity of the modified NK-92 cells.
- the invention is directed to methods for in-vitro assessment of the efficacy of an antibody to induce cell death.
- Such methods can include the steps of exposing a target cell to an antibody (monoclonal (purified or in hybridoma supernates), polyclonal, chimeric (such as one having at least two dissimilar antigen binding domains (wherein one binding domain can be adapted to bind the Fc receptor), or any other form of antibody), exposing the target cell to a modified NK-92 expressing an Fc receptor; and then monitoring the target cell for cytotoxicity, cytolysis, or apoptosis, or a combination thereof.
- Pluralities of cells and antibodies can be used.
- the target cells used in the methods can have a lysis or aptotic rate of about 5%-30% in the presence of the modified NK-92 cells in the absence of antibody.
- Effector:target ratios include 0.5:1 to 100:1, including 1:1 and 20:1.
- Target cells in the methods include SKOV-3, P815, THP-1, U373MG, T98G, A ML193, SR91, ALL1, and REH; these and any other target cells can be modified to increase expressiono f the antigen to which the antibody binds.
- Appropriate negative controls include using unmodified NK-92 cells.
- the NK-92 cells in this aspect can include those modified to express a Fc receptor on a surface of the cell;
- the Fc receptor can be an activating Fc ⁇ receptor, CD16 (Fc ⁇ RIII-A), or any member of an Fc receptor class, such as FC ⁇ RI (CD64), FC ⁇ RII (CD32), FC ⁇ RIII, FcRn, Fc ⁇ and Fc ⁇ .
- the Fc receptors can be of any binding affinity for their ligands, or fragments of their ligands, including low- and high-binding affinity forms.
- the NK-92 cells can be modified by introducing a polynucleotide that encodes a polypeptide having at least 70%, 80%, 90%, 95%, 99% or 100% identity to the amino acid sequences of SEQ ID NO:1 or SEQ ID NO:2; one such polynucleotide includes SEQ ID NO:3.
- the NK-92 cells can be further modified to express one or more associated accessory signaling polypeptides, cytokines, or fragments thereof; such expression can correlate with increased surface expression of the Fc receptor.
- Associated accessory signaling polypeptides include Fc ⁇ RI- ⁇ (SEQ ID NO 5) or TCR- ⁇ (SEQ ID NO:7). Expression of a cytokine (such as interleukin-2) can also correlate with viability or cytotoxicity of the modified NK-92 cells. Cytokines can also be added to the assay from exogenous sources.
- the invention is directed to methods for detecting cytolytic and apoptosis-inducing activity, the method including the steps of exposing a target cell in the absence of antibodies to a NK-92 cell expressing an Fc receptor, and then monitoring the target cell for cytotoxicity, cytolysis or apoptosis. Monitoring can include determining IFN- ⁇ or cytokine expression levels.
- the method can further include applying a blocking agents, such as activating receptor-masking antibodies or polypeptides (or fragments of these) to suppress one or more activating receptors on the NK-92 cell.
- the invention is directed to methods of assaying the efficacy of an antibody to treat a tumor, infection or other lesion, the method including the steps of administering an antibody (or plurality of antibodies) to a subject, administering modified NK-92 cells expressing an Fc receptor to the subject; and then monitoring the tumor, infection or lesion.
- the efficacy of the antibody in the treatment correlates with suppression of the tumor, infection or lesion in the subject.
- Monitoring can include determining IFN- ⁇ or cytokine expression levels.
- the method can further include applying a blocking agents, such as activating receptor-masking antibodies or polypeptides (or fragments of these) to suppress one or more activating receptors on the NK-92 cell.
- the antibody can be monoclonal (purified or in hybridoma supernates), polyclonal, chimeric (such as one having at least two dissimilar antigen binding domains (wherein one binding domain can be adapted to bind the Fc receptor), or any other form of antibody.
- Cytokines such as interleukin-2
- chimeric such as one having at least two dissimilar antigen binding domains (wherein one binding domain can be adapted to bind the Fc receptor), or any other form of antibody.
- Cytokines such as interleukin-2
- fragments thereof can be expressed from modified NK-92 cells or supplied exogenously.
- Subjects include bovines (e.g., cows), swine (e.g ., pigs, hogs), rabbits, alpacas, horses, canines (e.g., dogs), felines (e.g ., cats), ferrets, rats, mice, fowl (chickens, turkeys) and buffalo. Subjects can also be human.
- the NK-92 cells in this aspect can include those modified to express a Fc receptor on a surface of the cell;
- the Fc receptor can be an activating Fc ⁇ receptor, CD16 (Fc ⁇ RIII-A), or any member of an Fc receptor class, such as FC ⁇ RI (CD64), FC ⁇ RII (CD32), FC ⁇ RIII, FcRn, Fc ⁇ and Fc ⁇ .
- the Fc receptors can be of any binding affinity for their ligands, or fragments of their ligands, including low- and high-binding affinity forms.
- the NK-92 cells can be modified by introducing a polynucleotide that encodes a polypeptide having at least 70%, 80%, 90%, 95%, 99% or 100% identity to the amino acid sequences of SEQ ID NO:1 or SEQ ID NO:2; one such polynucleotide includes SEQ ID NO:3.
- the NK-92 cells can be further modified to express one or more associated accessory signaling polypeptides, cytokines, or fragments thereof; such expression can correlate with increased surface expression of the Fc receptor.
- Associated accessory signaling polypeptides include Fc ⁇ RI- ⁇ (SEQ ID NO:5)or TCR- ⁇ (SEQ ID NO:7).
- the invention is directed to methods of treating a subject, the subject having a tumor, infection or other lesion, the method including administering to a subject antibodies that specifically bind to the tumor, infection or other lesion; and then administering to the subject modified NK-92 cells expressing an Fc receptor.
- a reduction in the tumor, infection or lesion indicates a therapeutic response.
- Monitoring can include determining IFN- ⁇ or cytokine expression levels.
- the method can further include applying a blocking agents, such as activating receptor-masking antibodies or polypeptides (or fragments of these) to suppress one or more activating receptors on the NK-92 cell.
- the antibody can be monoclonal (purified or in hybridoma supernates), polyclonal, chimeric (such as one having at least two dissimilar antigen binding domains (wherein one binding domain can be adapted to bind the Fc receptor), or any other form of antibody.
- Cytokines (such as interleukin-2), or fragments thereof, can be expressed from modified NK-92 cells or supplied exogenously.
- Subjects include bovines (e.g., cows), swine (e.g., pigs, hogs), rabbits, alpacas, horses, canines ( e.g ., dogs), felines (e.g., cats), ferrets, rats, mice, fowl (chickens, turkeys) and buffalo. Subjects can also be human.
- the NK-92 cells in this aspect can include those modified to express a Fc receptor on a surface of the cell;
- the Fc receptor can be an activating Fc ⁇ receptor, CD 16 (Fc ⁇ RIII-A), or any member of an Fc receptor class, such as FC ⁇ RI (CD64), FC ⁇ RII (CD32), FC ⁇ RIII, FcRn, Fc ⁇ and Fc ⁇ .
- the Fc receptors can be of any binding affinity for their ligands, or fragments of their ligands, including low- and high-binding affinity forms.
- the NK-92 cells can be modified by introducing a polynucleotide that encodes a polypeptide having at least 70%, 80%, 90%, 95%, 99% or 100% identity to the amino acid sequences of SEQ ID NO:1 or SEQ ID NO:2; one such polynucleotide includes SEQ ID NO:3.
- the NK-92 cells can be further modified to express one or more associated accessory signaling polypeptides, cytokines, or fragments thereof; such expression can correlate with increased surface expression of the Fc receptor.
- Associated accessory signaling polypeptides include Fc ⁇ RI- ⁇ (SEQ ID NO:5)or TCR- ⁇ (SEQ ID NO:7).
- the present invention is directed towards cell lines and methods that potentiate and broaden the effective scope of the ADCC response.
- the present invention provides an NK-92 cell line that stably expresses an Fc cell surface receptor protein, such as CD 16.
- an Fc cell surface receptor protein such as CD 16.
- NK cells can, in turn, bind to the Fc (constant) region of these tumor-bound antibodies via the CD 16 receptors displayed on the NK cells and initiate lysis of the tumor cell through the ADCC mechanism.
- NK cell-mediated ADCC an essential part of the development of antibody-based cancer therapies is the in-vitro determination of the efficacy and specificity of NK cell-mediated ADCC that is imparted by the binding of the antibody to the target tumor cell.
- PBL peripheral blood lymphocytes
- NK cells isolated from the PBL blood fraction as effector cells.
- PBL peripheral blood lymphocytes
- allelic variations in the extracellular portion of the CD 16 gene can result in significant differences in CD 16 affinity for the Fc portions of antibodies and differences in the activation status of donor NK cells can alter the level of CD 16 expression on the cell surface.
- concentration of NK cells in the PBL fraction also varies, partly for genetic reasons and partly as a reflection of the physiological status of the donor. This effector cell variability greatly complicates the assessment of monoclonal antibodies as potential therapeutic agents.
- NK cells expressing the low binding affinity form of CD 16 are most common, the high affinity isotype is sufficiently common that antibody testing needs to be carried using NK cells of both forms (Koene et al., 1997).
- Identifying donors homozygous for low and high affinity allelic forms of CD16 is a difficult task.
- the availability of a clonal human NK cell population that expresses a consistent level of CD 16 activity would provide substantial benefit as a standard effector in the evaluation of antibodies for ADCC activity and specificity.
- NK cells having known high levels of Fc-binding capacity and cytotoxic activity can benefit from the presence of NK cells having known high levels of Fc-binding capacity and cytotoxic activity within the subject.
- NK cells isolated from cancer subjects are often found to have been rendered defective, deficient or ineffective by actions of the tumor cells.
- Some types of tumor cells for example, are able to kill or deactivate NK cells in a subject-specific manner.
- Other types of tumor cells similarly are able to interfere with NK cell production, activity and/or specificity.
- Such variability makes reliance on subject NK cells problematic in a therapeutic setting and suggests that the co-administration of known quantities of exogenous NK cells having a known level of activity along with an appropriate antibody can result in more consistent therapeutic effects.
- the availability of a clonal human NK cell population that expresses a consistent level of CD 16 activity is expected to provide substantial benefit.
- NK cells express a repertoire of cell surface receptors that, when bound to the corresponding MHC-I ligand on a normal target cell, strongly and specifically prevent destruction of the target cell by inhibiting NK cell activation, cytotoxicity and cytokine response. This inhibition can abrogate the activation of NK cells caused by the binding of NK cell activating receptors to their conjugate ligands on the target cell.
- a NK cell will destroy a target cell that displays only activating ligands, but will spare a target cell that displays MHC-I inhibitory ligands even if activating ligands are also present.
- MHC-I proteins have the primary function of displaying peptide antigens that are fragments derived from proteins expressed within a cell and are classified as being MHC-I complexes.
- the MHC complexes displayed on normal cells are unique to each individual and are often referred to as being markers of "self" for that individual.
- Exogenous cells introduced by transplantation display MHC molecules and associated peptides that differ from those of the host individual and are therefore referred to as being "non-self.”
- Non-self MHC-peptide complexes can also appear on aberrant cells as a result of processes that alter the peptides presented on the MHC molecules.
- non-self peptides are displayed by many, but not all, tumor cells and infected cells.
- NK cell inhibitory receptors consist of several families of proteins that recognize, bind to and are triggered to send "negative intracellular signals" by encountering intact self MHC-I proteins on the surface of a normal self, target cell. NK cells are therefore prevented from attacking and destroying normal cells that display the appropriate self MHC-I constellation. Tumor and infected cells that display this self MHC-I constellation are also immune from attack. Only cells that display non-self or no MHC-I are subject to destruction by NK cells. Some types of tumor and infected cells that do not display self MHC-I complexes have, however, evolved mechanisms that allow them to escape this fate.
- escape mechanisms include expression of surrogate MHC-I-like, NK cell inhibitory receptor ligands and the secretion of soluble ligands that suppress NK cell functions. Tumor and infected cells that implement such escape mechanisms are refractory to NK cell-mediated lysis. The efficacy of NK cells as an agent for the destruction of cancer cells is therefore limited by the presence of appropriate MHC-I ligands for NK cell inhibitory receptors. The availability of a human NK cell population that does not express NK cell inhibitory receptors would beneficially expand the range of cancers and infections that can be treated using antibody-based therapeutic agents.
- NK-92 is a NK-like cell line that was initially isolated from the blood of a subject suffering from a large granular lymphoma and subsequently propagated in cell culture.
- the NK-92 cell line has been described (Gong et al ., 1994; Klingemann, 2002).
- NK-92 cells determined have a CD3-/CD56+ phenotype that is characteristic of NK cells. They express all of the known NK cell-activating receptors except CD16, but lack all of the known NK cell inhibitory receptors except NKG2A/CD94 and ILT2/LIR1, which are expressed at low levels.
- NK-92 is a clonal cell line that, unlike the polyclonal NK cells isolated from blood, expresses these receptors in a consistent manner with respect to both type and cell surface concentration.
- NK-92 cells are not immunogenic and do not elicit an immune rejection response when administered therapeutically to a human subject. Indeed NK-92 cells are well tolerated in humans with no known detrimental effects on normal tissues.
- NK-92 cells unlike NK cells and cells of most of the other known NK-like cell lines, have been engineered to express novel proteins by means of transduction using retroviral vectors (Campbell et al ., 2004; Kikuchi-Maki et al ., 2003; Klingemann, 2002; Yusa and Campbell, 2003; Yusa et al ., 2002; Yusa et al., 2004), such engineering has proved difficult as evidenced by numerous failures to engineer NK-92 cells to express an Fc receptor. More particularly, despite the clear potential benefits which could be anticipated from an NK-92 cell line modified to express CD16, such genetic modification had not been achieved in fact until the present invention.
- NK-92 as a suitable platform upon which the present invention can be constructed.
- the lack of inhibitory receptors means that NK-92 are not MHC-restricted and can act effectively against any cell that displays an appropriate activating ligand independent of any MHC-I inhibitory ligands that can also be expressed.
- the lack of immunogenicity coupled with the relative ease with which NK-92 cells can be grown in culture means that they can be prepared in bulk and administered to any subject as the need arises.
- the stability and consistency of NK-92 makes it suitable for use as a reference material and therapeutic agent.
- the present invention provides the ability to transduce NK-92 with genes for novel proteins, such as Fc receptors, in conjunction with the ability of NK-92 to stably express these proteins, as explained in greater detail below.
- NK-92 cells as a therapy for cancers is currently being evaluated with promising results in human clinical trials.
- the benefits of NK-92 cells are being further exploited through the development of genetically engineered NK-92 variants that express an protein construct that covalently links an antibody-like binding domain to a signaling domain such as TCR- ⁇ (Genbank Accession No. J04132; SEQ ID NO:6) (TCR- ⁇ (Genbank Accession No. J04132; SEQ ID NO:6)) (Klingemann, 2002; Maki et al., 2001; Uherek et al., 2001; Uherek et al., 2002).
- the antibody-like domain is structured to specifically bind to an antigen that is expressed by a target cell while the signaling domain is one that is known to trigger NK and NK-92 cell activity when stimulated. It has, to date, been demonstrated in-vitro and in animal models that the binding of the antibody-like domain of such a construct to its antigen on a target cell triggers the NK-92 cell in a manner such that it rapidly and efficiently destroys the target cell via direct conjugation.
- the utility of these constructs as therapeutic agents is, however, limited by the need to design, prepare and validate a unique construct for each specific type of cancer or infection to be treated. The availability of a single NK-92 variant that can be used to treat a broad range of cancers and infections is of beneficial utility.
- NK-92 cells can be improved in subjects, in that the cytotoxicity, cell surface receptor concentration and survival of NK-92 cells as well as the range of tumor and infected cell types that are attacked have been shown to be increased by the presence of low concentrations of the cytokine interleukin-2 (IL-2).
- IL-2 cytokine interleukin-2
- the cost of the exogenously added IL-2 needed to maintain and expand NK-92 in commercial scale culture is significant, while the administration of IL-2 to human subjects in sufficient quantity to achieve the desired effects is also known to cause adverse side effects.
- NK-92 cells Another area in which NK-92 cells can be improved, and the focus of the present invention, concerns the fact that unmodified NK-92 does not express CD16 and therefore is ineffective in killing target cells via the ADCC mechanism.
- NK-92 cells are widely used as a model system for the study of NK cell activation, action and inhibition, the lack of CD 16 expression precludes the use of NK-92 cells for the evaluation of efficacy of antibodies as therapeutic agents and the use of NK-92 as a therapeutic agent that is co-administered with an antibody.
- the present invention addresses this limitation by causing NK-92 cells to express CD16. Additional utility and benefit of the present invention will become apparent in the following descriptions.
- CD16 is most commonly found in a form that has a relatively low binding affinity for the Fc portion of IgG molecules.
- An alternative form that exhibits a higher binding affinity is found in some individuals.
- the low and high affinity forms of CD16 differ only by the substitution of valine (high affinity) for phenylalanine (low affinity) at position 157 in the polypeptide chain.
- the complete sequences of the low and high affinity forms can be found in the SwissProt database as entries P08637(SEQ ID NO:1) and VAR_008801 (SEQ ID NO:2), respectively and are presented in Tables 1 and 2; the polynucleotide encoding SEQ ID NO:1 (SEQ ID NO:3) is presented in Table 3.
- CD 16 was introduced into NK-92 cells by means of retroviral transduction in the following manner.
- Complementary DNA encoding the gene for either the low or high affinity form of CD 16 was sub-cloned into a bi-cistronic retroviral expression vector, pBMN-IRES-EGFP (obtained from G. Nolan, Stanford University, Stanford, CA) using the Bam HI and Not I restriction sites in accordance with standard methods (e.g., (Ausubel, 2002; Sambrook and Russell, 2001)).
- This expression vector was then transfected into the Phoenix-Amphotropic retroviral packaging cell line and the resulting virus-containing supernate was used to transduce NK-92 cells, although alternative methods including those in which vectors incorporate EGFP or other fluorescent proteins (yellow, red, cyan, etc.) can be used without departing from the spirit and scope of this invention, and the Phoenix-Amphotropic retroviral packaging cell line were both obtained from and are available to the public from the Leland Stanford University, Stanford, California, USA; (Kinsella and Nolan, 1996; Nolan and Kinsella, 1998)). As indicated below, other vectors and packaging cell lines, both those currently known and those which can be developed in the future, can be used.
- NK-92-CD16 Transduced NK-92 cells expressing CD16 on their surface
- FACS fluorescence activated cell sorter
- the NK-92-CD16 cells were further sub-sorted on the basis of CD16 expression level using a FACS, based upon coordinate expression of Enhanced Green Fluorescent Protein (EGFP).
- EGFP Enhanced Green Fluorescent Protein
- Vectors are tools used to shuttle DNA between host cells or as a means to express a polynucleotide sequence. Inserting the DNA of interest, such as a CD16 sequence or a fragment, is accomplished by ligation techniques and/or mating protocols well known to the skilled artisan. Such DNA is inserted such that its integration does not disrupt any necessary components of the vector. In the case of vectors that are used to express the inserted DNA as a polypeptide, the introduced DNA is operably-linked to the vector elements that govern its transcription and translation.
- Vectors can be divided into two general classes: Cloning vectors are replicating plasmid or phage with regions that are non-essential for propagation in an appropriate host cell, and into which foreign DNA can be inserted; the foreign DNA is replicated and propagated as if it were a component of the vector.
- An expression vector (such as a plasmid, yeast, or animal virus genome) is used to introduce foreign genetic material into a host cell or tissue in order to transcribe and translate the foreign DNA.
- the introduced DNA is operably-linked to elements, such as promoters, that signal to the host cell to transcribe the inserted DNA.
- Some promoters are exceptionally useful, such as inducible promoters that control gene transcription in response to specific factors.
- Operably-linking a CD16 polynucleotide to an inducible promoter can control the expression of a CD16 gene or fragments.
- inducible promoters include those that are tissue-specific, which relegate expression to certain cell types, steroid-responsive (e.g., glucocorticoids (Kaufman, 1990)and tetracycline), or heat-shock reactive. Some bacterial repression systems, such as the lac operon, have been exploited in mammalian cells and transgenic animals (Fieck et al., 1992; Wyborski et al., 1996; Wyborski and Short, 1991).
- Other desirable inducible promoters include those that are not endogenous to the cells in which the construct is being introduced, but, however, are responsive in those cells when the induction agent is exogenously supplied.
- Vectors have many manifestations.
- a "plasmid” is a circular double stranded DNA molecule that can accept additional DNA fragments. Viral vectors can also accept additional DNA segments into the viral genome.
- Certain vectors are capable of autonomous replication in a host cell (e.g., bacterial vectors having a bacterial origin of replication and episomal mammalian vectors). Other vectors (e.g., non-episomal mammalian vectors) integrate into the genome of a host cell and replicate as part of the host genome.
- useful expression vectors are plasmids and viral vectors (e.g. , replication defective retroviruses, adenoviruses and adeno-associated viruses); other expression vectors can also be used.
- Vector choice is dictated by the organisms or cells being used and the desired fate of the vector.
- Vectors can replicate once in the target cells, or can be "suicide" vectors.
- vectors comprise signal sequences, origins of replication, marker genes, enhancer elements, promoters, and transcription termination sequences.
- Vectors often use a selectable marker to facilitate identifying those cells that have incorporated the vector. Table F summarizes many of the available markers.
- “Host cell” and “recombinant host cell” are used interchangeably. Such terms refer not only to a particular subject cell but also to the progeny or potential progeny of such a cell. Because certain modifications may occur in succeeding generations due to either mutation or environmental influences, such progeny may not, in fact, be identical to the parent cell, but are still included within the scope of the term.
- eukaryotic cell transfection and prokaryotic cell transformation are well known in the art (see examples in Table B).
- the choice of host cell dictates the preferred technique for introducing the polynucleotide of interest.
- Introduction of polynucleotides into an organism may also be done with ex vivo techniques that use an in vitro method of transfection, as well as established genetic techniques, if any, for that particular organisms.
- Such procedures can similarly be employed for the transduction of genetically engineered NK-92 cells, including NK-92-CD16- ⁇ , NK-92-CD16- ⁇ , NK-92mi and NK-92ci.
- NK-92, NK-92mi and NK-92ci cell lines are deposited with the American Type Culture Collection under Deposit Numbers CRL-2407, CRL-2408 and CRL-2409, respectively.
- NK-92-CD16, NK-92-CD16- ⁇ , NK-92-CD16- ⁇ and NK-92-CD16(F 157V) are being submitted to the American Type Culture Collection..
- BES N,N- bis(2-hydroxyethyl)-2-aminoethanesulfonic acid
- buffered solution Ishiura et al ., 1982
- Diethylaminoethyl (DEAE)-Dextran transfection Fujita et al ., 1986; Lopata et al ., 1984; Selden et al ., 1986
- Chloroquine can be used to increase efficiency.
- Electroporation Neuroporation (Neumann et al ., 1982; Potter, 1988; Potter et al ., 1984; Wong and Neumann, 1982) Especially useful for hard-to-transfect lymphocytes.
- Retroviral Production exemplified by (Cepko et al ., 1984; Miller and Buttimore, 1986; Pear et al ., 1993) Infection in vitro and in vivo : (Austin and Cepko, 1990; Bodine et al ., 1991; Fekete and Cepko, 1993; Koehne et al., 2003; Lemischka et al., 1986; Turner et al ., 1990) Lengthy process, many packaging lines available at ATCC. Applicable to both in vivo and in vitro transfection.
- NK-92 cells Other vectors and packaging cell lines have been used in the preparation of genetically modified variants of NK-92 cells (Klingemann, 2002; Nagashima et al., 1998; Tam et al., 1999; Uherek et al., 2002) and can be used equivalently herein. Retroviral transduction systems other than those of the Examples discussed below have also been successfully used to transduce a variety of genes into NK-92 cells.
- these alternative methods include, but are not limited to the p-JET vector in conjunction with FLYA13 packaging cells (Gerstmayer et al., 1999), the plasmid-based kat retroviral transduction system, and DFG-hIL-2-neo/CRIP (Nagashima et al., 1998). Electroporation and "gene gun" introduction of the vector into the packaging cells is also practiced.
- pBMN-IRES-EGFP vector in combination with the Phoenix-Amphotropic packaging cell line is convenient for the purpose of this and the following Examples in that it provides high efficiencies of Phoenix-Amphotropic cell transfection; the use of Moloney LTR promoters results in a high level of CD16 expression; the virus is produced at high titers; the efficiency of NK-92 transduction is improved over other vectors that have been used to transduce NK-92; and the vector provides adequate space to accommodate the CD16 cDNA or alternative inserts.
- the pBMN-IRES-EGFP vector further incorporates genes for enhanced green fluorescent protein (EGFP), which can be used as an endogenous surrogate marker for gene expression.
- EGFP enhanced green fluorescent protein
- the Phoenix cell line stably expresses this vector in episomal form along with producing other viral components, thus allowing the cells to stably produce virus for an extended period of time.
- previously described publications Karl, 2002; Nagashima et al., 1998; Tam et al., 1999; Uherek et al., 2002
- alternative retroviral systems can be used to introduce cDNAs into NK-92 without departing from the spirit and scope of the invention.
- a “homologous polynucleotide sequence” or “homologous amino acid sequence,” or variations thereof, refer to sequences characterized by a homology at the polynucleotide level or amino acid level.
- Homologous polynucleotide sequences encode those sequences coding for isoforms of CD16. Different genes can encode isoforms such as homologous CD16 polynucleotide sequences of species other than mice, including other vertebrates, such as human, frog, rat, rabbit, dog, cat, cow, horse, and other organisms.
- Homologous polynucleotide sequences also include naturally occurring allelic variations and mutations of SEQ ID NOs:1 or 2.
- Homologous polynucleotide sequences may encode conservative amino acid substitutions in SEQ ID NOS:1 or 2.
- the invention further encompasses using CD16 polynucleotide molecules that differ from the polynucleotide sequence shown in SEQ ID NO:3, due to degeneracy of the genetic code and thus encode same CD 16 as that encoded by the polynucleotide sequence shown in SEQ ID NOS:3.
- Any polynucleotide molecule encoding a polypeptide having an amino acid sequence shown in SEQ ID NOS:1 or 2 is useful for modifying NK-92 cells.
- DNA sequence polymorphisms that change the CD16 amino acid sequences can also be useful to modify NK-92 cells.
- allelic variations among individuals exhibit genetic polymorphisms in CD 16 genes.
- CD16 genes from other species that have a polynucleotide sequence that differs from the sequence of SEQ ID NO:3 are contemplated to be useful in the compositions and methods of the invention.
- CD16 variant polynucleotide or “CD16 variant polynucleotide sequence” means a polynucleotide molecule which encodes a CD16 polypeptide that (1) has at least about 70% polynucleotide sequence identity with a polynucleotide acid sequence encoding a full-length native CD16, (2) a full-length native CD16 lacking the signal peptide, (3) an extracellular domain of a CD16, with or without the signal peptide, or (4) any other fragment of a full-length CD16.
- a CD16 variant polynucleotide will have at least about 70% polynucleotide sequence identity, more preferably at least about 71% - 99% polynucleotide sequence identity and yet more preferably at least about 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% and even more preferably, 99% polynucleotide sequence identity with the polynucleotide sequence encoding a full-length, native CD16.
- a CD16 variant polynucleotide can encode full-length native CD16 lacking the signal peptide, an extracellular domain of CD 16, with or without the signal sequence, or any other fragment of a full-length CD16.
- CD16 variants are at least about 30 polynucleotides, often at least about 60, 90, 120, 150, 180, 210, 240, 270, 300, 450, 600 polynucleotides in length, more often at least about 900 polynucleotides in length, or more.
- Percent (%) polynucleotide sequence identity with respect to CD16-encoding polynucleotide sequences is defined as the percentage of polynucleotides in the CD 16 polynucleotide sequence of interest that are identical with the polynucleotides in a candidate sequence, after aligning the sequences and introducing gaps, if necessary, to achieve the maximum percent sequence identity. Alignment can be achieved in various ways well-known in the art; for instance, using publicly available software such as BLAST, BLAST-2, ALIGN or Megalign (DNASTAR) software. Those skilled in the art can determine appropriate parameters for measuring alignment, including any necessary algorithms to achieve maximal alignment over the full length of the sequences being compared.
- the % polynucleotide sequence identity of C to D will not equal the % polynucleotide sequence identity of D to C.
- Homologs or other related sequences can be obtained by low, moderate or high stringency hybridization with all or a portion of the particular sequence used as a probe using polynucleotide hybridization and cloning methods well known in the art.
- allelic variants of CD 16 polynucleotides changes can be introduced by mutation into SEQ ID NO:3 that incur alterations in the amino acid sequence of CD16 but does not alter CD16 function for the purposes of the invention.
- polynucleotide substitutions leading to amino acid substitutions at "non-essential" amino acid residues can be made in SEQ ID NOs:1 or 2.
- a "non-essential” amino acid residue is a residue that can be altered from the wild-type sequence of CD 16 without altering CD16 function in the methods and compositions of the invention, whereas an "essential" amino acid residue is required for activity.
- amino acid residues that are conserved among the CD 16 amino acids of the invention are particularly non-amenable to alteration (Table 9).
- substitutions Ala (A) Val, Leu, He Val Arg (R) Lys, Gln, Asn Lys Asn (N) Gln, His, Lys, Arg Gln Asp (D) Glu Glu Cys (C) Ser Ser Gln (Q) Asn Asn Glu (E) Asp Asp Gly (G) Pro, Ala Ala His (H) Asn, Gln, Lys, Arg Arg Ile (I) Leu, Val, Met, Ala, Phe, Norleucine Leu Leu (L) Norleucine, Ile, Val, Met, Ala, Phe Ile Lys (K) Arg, Gln, Asn Arg Met (M) Leu, Phe, He Leu Phe (F) Leu, Val, Ile, Ala, Tyr Leu Pro (P) Ala Ala Ser (S) Thr Thr Thr (T) Ser Ser Trp (W) Tyr, Phe
- Non-conservative substitutions that affect (1) the structure of the polypeptide backbone, such as a ⁇ -sheet or ⁇ -helical conformation, (2) the charge or (3) hydrophobicity, or (4) the bulk of the side chain of the target site can modify CD16 polypeptide function or immunological identity.
- Residues are divided into groups based on common side-chain properties as denoted in Table A.
- Non-conservative substitutions entail exchanging a member of one of these classes for another class. Substitutions may be introduced into conservative substitution sites or more preferably into non-conserved sites.
- the variant polypeptides can be made using methods known in the art such as oligonucleotide-mediated (site-directed) mutagenesis, alanine scanning, and PCR mutagenesis.
- Site-directed mutagenesis Carter, 1986; Zoller and Smith, 1987
- cassette mutagenesis restriction selection mutagenesis
- Wells et al., 1985 or other known techniques can be performed on the cloned DNA to produce CD16 variants (Ausubel, 2002; Sambrook and Russell, 2001).
- CD16 polypeptide variant means a CD16 polypeptide having at least: (1) about 80% amino acid sequence identity with a full-length native CD16 sequence, (2) a CD16 sequence lacking a signal peptide, (3) an extracellular domain of a CD16, with or without a signal peptide, or (4) any other fragment of a full-length CD16 sequence.
- CD16 variants include those wherein one or more amino acid residues are added or deleted at the Nor C- terminus of the full-length native amino acid sequence.
- a CD16 polypeptide variant will have at least about 80% amino acid sequence identity, preferably at least about 81% amino acid sequence identity, more preferably at least about 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% amino acid sequence identity and most preferably at least about 99% amino acid sequence identity with a full-length native sequence CD16 sequence.
- CD 16 variant polypeptides are at least about 10 amino acids in length, often at least about 20 amino acids in length, more often at least about 30, 40, 50, 60, 70, 80, 90, 100,150, 200, or 300 amino acids in length, or more.
- Percent (%) amino acid sequence identity is defined as the percentage of amino acid residues that are identical with amino acid residues in a CD 16 sequence in a candidate sequence when the two sequences are aligned. To determine % amino acid identity, sequences are aligned and if necessary, gaps are introduced to achieve the maximum % sequence identity; conservative substitutions are not considered as part of the sequence identity. Amino acid sequence alignment procedures to determine percent identity are well known to those of skill in the art. Publicly available computer software such as BLAST, BLAST2, ALIGN2 or Megalign (DNASTAR) can be used to align polypeptide sequences. Those skilled in the art will determine appropriate parameters for measuring alignment, including any algorithms needed to achieve maximal alignment over the full length of the sequences being compared.
- % amino acid sequence identity X / Y ⁇ 100
- the % amino acid sequence identity of A to B will not equal the % amino acid sequence identity of B to A.
- a CD 16 "chimeric polypeptide” or “fusion polypeptide” comprises CD16 fused to a non-CD 16 polypeptide.
- a non-CD 16 polypeptide is not substantially homologous to CD16 (SEQ ID NOs:1 or 2).
- a CD16 fusion polypeptide may include any portion to an entire CD 16, including any number of biologically active portions.
- Fusion polypeptides can be easily created using recombinant methods.
- a polynucleotide encoding CD16 (e.g., SEQ ID NO:3) can be fused in-frame with a non-CD16 encoding polynucleotide, to the CD16 N- or C- -terminus, or internally.
- Fusion genes may also be synthesized by conventional techniques, including automated DNA synthesizers and PCR amplification using anchor primers that give rise to complementary overhangs between two consecutive gene fragments that can subsequently be annealed and reamplified to generate a chimeric gene sequence (Ausubel, 2002).
- Many vectors are commercially available that facilitate sub-cloning CD16 in-frame to a fusion moiety.
- NK-92-CD16 cells can be used in ADCC assays as a pure "effector" cell population having defined and consistent characteristics. In some instances it can be desirable to select and use cells that exhibit intermediate levels of CD16 expression. In particular, such intermediate cells can be of use in generating dose-response curves and as "ladder" type calibrators for CD16 activity. NK-92 cells transduced with the low and high affinity forms of CD16 could likewise be used for these purposes.
- ADCC assays are typically performed by loading target cells with an indicator material such as [ 51 Cr] or a Europium chelate; treating the indicator-loaded target cells with the antibody to be evaluated; and exposing these cells to NK-92-CD16 effector cells. Lysis of the target cells is indicated by the release of the indicator material into the assay supernate where its concentration can be measured by a suitable method such as scintillation counting ( 51 Cr) or fluorescence intensity or lifetime determination (Europium chelate).
- an indicator material such as [ 51 Cr] or a Europium chelate
- 51 Cr scintillation counting
- Europium chelate fluorescence intensity or lifetime determination
- Efficacy can be likewise be assessed by the measurement of surrogate indicators such as cytokine release by the NK-92-CD 16 cells; the up-regulation ofNK cell activation markers, such as CD25, CD69 and/or CD95L; activation of NK-92 cell transcription factors, such as NF-AT or NF- ⁇ B; or the activation of caspases or other markers of apoptosis in the target cells.
- CD 16-deficient parental NK-92 cells serve as a unique and valuable control in such assays as they permit differentiating between ADCC-mediated cytotoxicity and other cytolytic effects that NK-92 cells exert on the target cells.
- the preferred target cells in ADCC assays are ones that express an antigen that is appropriate to the antibody being evaluated and that have low susceptibility to lysis by the parental NK-92 cell line. If such a target cell line is not conveniently available, other suitable cell lines, such as the ovarian carcinoma line SKOV-3 (e.g., ATCC Deposit HTB-77) (Tam et al ., 1999), can sometimes be used as a viable substitute, particularly if transduced/transfected such that they express the specific antigen required.
- SKOV-3 e.g., ATCC Deposit HTB-77
- NK-92 Fc ⁇ RII/III + myelocytic leukemia line THP-1 (e.g., ATCC Deposit No. TIB-202) that have limited (between 5 and 30%) susceptibility to lysis by unmodified NK-92 cells are preferably used where redirected cytotoxicity or ADCC is to be determined in order to ensure sufficient assay dynamic range for the detection of significant effects through CD16.
- Other cell types with limited cytolytic potential that express or are engineered to express specific cell surface markers of interest can also be employed as targets.
- the baseline cytolytic capacity of NK-92 can be reduced by either decreasing the IL-2 concentration in the cultures and/or assaying four days after passing the cells into fresh IL-2-containing medium.
- CD 16 introduced into NK-92-CD16, NK-92-CD16- ⁇ or NK-92-CD16- ⁇ cells can be determined using the cytotoxicity assay of Example 4 in either the ADCC or the "redirected cytotoxicity" format.
- Monoclonal antibodies that bind CD16 can be used to test for function of the receptor on NK-92 cells in a redirected cytotoxicity assay, in which the antibody's F(ab) portion binds the receptor on the NK cell and the Fc portion binds to Fc receptors on appropriate target cells (Fc ⁇ RII/III on P815 or THP-1 target cells).
- Another form of redirected cytotoxicity can be tested using a chimeric bi-specific antibody, such as 2B1 (Clark et al., 1997; Weiner et al., 1995a; Weiner et al., 1995b), which expresses two F(ab) regions, one which binds CD16 on the NK-92 cell and another that binds the Her2/neu antigen on an appropriate target cell line, such as SKOV-3.
- monoclonal antibodies that specifically bind antigens that are uniquely expressed on the target cells can directly test ADCC.
- the F(ab) portion of the antibody binds to the corresponding ligand on the target cell while the CD16 receptor on the NK-92-CD16 cells bind to the Fc portion of the antibody.
- the resulting cross-link between the antigen on the target cell and the CD16 receptor results in lysis of the target cell via the ADCC pathway.
- a bi-functional antibody having one domain that specifically binds to an antigen of interest on the target cells and a second domain that specifically binds to CD16 on NK-92-CD16 cells can be evaluated in the manner described above.
- the bi-functional antibody cross-links the antigen on the target cell to CD16 on the NK-92-CD16 cell and triggers an ADCC response.
- the same assay for research purposes can, for example, treat a target cell that expresses CD16 or another Fc receptor with an antibody such as anti-CD16 that is directed against this receptor. Exposing the anti-CD16 labeled target cells to NK-92-CD16 cells results in the cross-linking of the receptors on both cells with consequent triggering of ADCC. Differentiation between the ADCC and redirected cytotoxicity formats is based upon whether the effector cell CD 16 receptor binds to the Fc portion of an antibody (ADCC) or this same receptor is bound by the F(ab) portion of an anti-CD 16 antibody (redirected cytotoxicity). As both binding arrangements can trigger similar cytotoxicity responses in the target cell, the choice between the ADCC and redirected formats is largely a matter of convenience.
- NK-92 cells it can be advantageous to block known activating receptors on NK-92 cells; such methods and agents are well-known; see for example (Pende et al., 1999; Pessino et al., 1998; Vitale et al., 1998).
- masking antibodies can be used (Pessino et al., 1998).
- NK-92-CD16 cells can effectively and efficiently lyse target cells.
- CD 16 in NK cells is non-covalently associated in the plasma membrane with homodimers or heterodimers of the Fc ⁇ RI- ⁇ (Genbank Accession No. M33195; SEQ ID NO:4 (polynucleotide) and SEQ ID NO:5 (polypeptide)) or TCR- ⁇ (Genbank Accession No. J04132; SEQ ID NO:6 (polynucleotide); SEQ ID NO:7 (polypeptide)) accessory signaling proteins; these sequences are presented in Tables 4-7.
- sequence identity applies also to SEQ ID NOs:4-7; thus, those polynucleotides or polypeptides of SEQ ID NOs:4-7 having about at least 70%-100% sequence identity, as well as 80%-90%, and 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% and 99% sequence identity are useful for the methods and composition of the invention.
- these accessory signaling proteins can transduce intracellular signals that activate NK cell cytotoxicity and cytokine release activities. In addition, they support surface expression of CD 16.
- Fc ⁇ RI- ⁇ and/or TCR- ⁇ can conveniently be co-introduced into NK-92 cells by sequential transduction with CD16 and Fc ⁇ RI- ⁇ and/or TCR- ⁇ cDNA in the manner described above. In this process, it is generally desirable to delete the EGFP gene from the vector containing the CD16 cDNA.
- the sequential transduction process consists of transducing the parental NK-92 cells with the CD 16 vector; immunostaining the transduced cells with a fluorescently labeled anti-CD 16 antibody; sorting the cells for CD 16 expression; transducing the NK-92-CD16 cells with a vector containing cDNA for both the accessory protein and EGFP; and sorting the doubly transduced cells on the basis of EGFP expression.
- the resulting doubly transduced NK-92 cells (NK-92-CD16/ ⁇ or NK-92-CD16/ ⁇ , respectively)
- NK-92 cells are widely used as a model system for the study of NK cell activation, action and inhibition as they stably express a defined suite of known NK cell activating receptors including NKp46, NKp44, 2B4, and NKG2D, but lacking CD 16, activating KIR, and NKG2C. More importantly, they also lack almost all of the known NK cell inhibitory receptors except low levels of NKG2A/CD94 and ILT2/LIR1. This is a major advantage of the present invention since MHC class I molecules, which are expressed on most cells and serve as ligands for NK cell inhibitory receptors do not effectively inhibit the activation of NK-92 cells.
- the present invention restores the CD16 activating receptor to NK-92 cells thereby increasing the range of activating ligands to which these cells respond.
- Both the activating receptors and any residual inhibitory receptors can be selectively blocked by the treatment of the effector cells with the appropriate monoclonal antibodies or the corresponding F(ab')2 fragments, such as 3.43.13 (anti-NKp44), 9E2 (anti-NKp46), 158 (anti-2B4), and 3G8 (anti-CD16).
- the ability to selectively block individual receptors or groups of receptors in conjunction with target cells that differ in susceptibility to lysis by NK-92 cells (and derivatives thereof) facilitates the study of the many mechanisms involved in NK cell activation and inhibition.
- the invention makes use of Abs and antibody fragments, such as F ab or (F ab ) 2 , that bind immunospecifically to their epitopes.
- Antibody comprises single Abs directed against an epitope, anti- Ab compositions with poly-epitope specificity, single chain anti-Abs, and fragments of Abs.
- a "monoclonal antibody” is obtained from a population of substantially homogeneous Abs, i.e., the individual Abs comprising the population are identical except for possible naturally-occurring mutations that may be present in minor amounts.
- Exemplary Abs include polyclonal (pAb), monoclonal (mAb), humanized, bi-specific (bsAb), chimeric and heteroconjugate Abs.
- Antibodies can be produced by any known method in the art or obtained commercially.
- the Abs may be monovalent Abs that consequently do not cross-link with each other.
- one method involves recombinant expression of immunoglobulin (Ig) light chain and modified heavy chains. Heavy chain truncations generally at any point in the F c region will prevent heavy chain cross-linking. Alternatively, the relevant cysteine residues are substituted with another amino acid residue or are deleted, preventing cross-linking. In-vitro methods are also suitable for preparing monovalent Abs. Abs can be digested to produce fragments, such as F ab fragments (Harlow and Lane, 1988; Harlow and Lane, 1999).
- Abs may further comprise humanized or human Abs.
- Humanized forms of non-human Abs are chimeric Igs, Ig chains or fragments (such as F v , F ab , F ab' , F (ab')2 or other antigen-binding subsequences of Abs) that contain minimal sequence derived from non-human Ig.
- a humanized antibody has one or more amino acid residues introduced from a non-human source. These non-human amino acid residues are often referred to as "import" residues, which are typically taken from an "import” variable domain. Humanization is accomplished by substituting rodent CDRs or CDR sequences for the corresponding sequences of a human antibody (Jones et al ., 1986; Riechmann et al., 1988; Verhoeyen et al., 1988). Such "humanized” Abs are chimeric Abs (1989), wherein substantially less than an intact human variable domain has been substituted by the corresponding sequence from a non-human species.
- humanized Abs are typically human Abs in which some CDR residues and possibly some FR residues are substituted by residues from analogous sites in rodent Abs.
- Humanized Abs include human Igs (recipient antibody) in which residues from a complementary determining region (CDR) of the recipient are replaced by residues from a CDR of a non-human species (donor antibody) such as mouse, rat or rabbit, having the desired specificity, affinity and capacity.
- donor antibody such as mouse, rat or rabbit
- corresponding non-human residues replace F v framework residues of the human Ig.
- Humanized Abs may comprise residues that are found neither in the recipient antibody nor in the imported CDR or framework sequences.
- the humanized antibody comprises substantially all of at least one, and typically two, variable domains, in which most if not all of the CDR regions correspond to those of a non-human Ig and most if not all of the FR regions are those of a human Ig consensus sequence.
- the humanized antibody optimally also comprises at least a portion of an Ig constant region (F c ), typically that of a human Ig (Jones et al., 1986; Presta, 1992; Riechmann et al ., 1988).
- Human Abs can also be produced using various techniques, including phage display libraries (Hoogenboom et al., 1991; Marks et al., 1991) and the preparation of human mAbs (Boerner et al., 1991; Reisfeld and Sell, 1985). Similarly, introducing human Ig genes into transgenic animals in which the endogenous Ig genes have been partially or completely inactivated can be exploited to synthesize human Abs.
- Bi-specific Abs are monoclonal, preferably human or humanized, that have binding specificities for at least two different antigens.
- bi-specific Abs is based on the co-expression of two Ig heavy-chain/light-chain pairs, where the two heavy chains have different specificities (Milstein and Cuello, 1983). Because of the random assortment of Ig heavy and light chains, the resulting hybridomas (quadromas) produce a potential mixture of ten different antibody molecules, of which only one has the desired bi-specific structure.
- the desired antibody can be purified using affinity chromatography or other techniques (Traunecker et al ., 1991; 1993).
- variable domains with the desired antibody-antigen combining sites are fused to Ig constant domain sequences.
- the fusion is preferably with an Ig heavy-chain constant domain, comprising at least part of the hinge, CH2, and CH3 regions.
- the first heavy-chain constant region (CH1) containing the site necessary for light-chain binding is in at least one of the fusions.
- the interface between a pair of antibody molecules can be engineered to maximize the percentage of heterodimers that are recovered from recombinant cell culture (1996).
- the preferred interface comprises at least part of the CH3 region of an antibody constant domain.
- one or more small amino acid side chains from the interface of the first antibody molecule are replaced with larger side chains (e.g. tyrosine or tryptophan).
- Compensatory "cavities" of identical or similar size to the large side chain(s) are created on the interface of the second antibody molecule by replacing large amino acid side chains with smaller ones (e.g. alanine or threonine). This mechanism increases the yield of the heterodimer over unwanted end products such as homodimers.
- Bi-specific Abs can be prepared as full length Abs or antibody fragments (e.g. F (ab')2 bi-specific Abs).
- F (ab')2 bi-specific Abs One technique to generate bi-specific Abs exploits chemical linkage.
- Intact Abs can be proteolytically cleaved to generate F (ab')2 fragments (Brennan et al ., 1985). Fragments are reduced with a dithiol complexing agent, such as sodium arsenite, to stabilize vicinal dithiols and prevent intermolecular disulfide formation. The generated F ab' fragments are then converted to thionitrobenzoate (TNB) derivatives.
- TBN thionitrobenzoate
- One of the F ab' -TNB derivatives is then reconverted to the F ab' -thiol by reduction with mercaptoethylamine and is mixed with an equimolar amount of the other F ab' -TNB derivative to form the bi-specific antibody.
- the produced bi-specific Abs can be used as agents for the selective immobilization of enzymes.
- F ab' fragments may be directly recovered from E. coli and chemically coupled to form bi-specific Abs.
- bi-specific F (ab')2 Abs can be produced (Shalaby et al., 1992).
- Each F ab' fragment is separately secreted from E. coli and directly coupled chemically in-vitro, forming the bi-specific antibody.
- the fragments comprise a heavy-chain variable domain (V H ) connected to a light-chain variable domain (V L ) by a linker that is too short to allow pairing between the two domains on the same chain.
- V H and V L domains of one fragment are forced to pair with the complementary V L and V H domains of another fragment, forming two antigen-binding sites.
- Another strategy for making bi-specific antibody fragments is the use of single-chain F v (sF v ) dimers (Gruber et al., 1994). Abs with more than two valencies are also contemplated, such as tri-specific Abs (Tutt et al., 1991).
- Heteroconjugate Abs consisting of two covalently joined Abs, have been proposed to target immune system cells to unwanted cells (1987) and for treatment of human immunodeficiency virus (HIV) infection (1991; 1992).
- immunotoxins may be constructed using a disulfide exchange reaction or by forming a thioether bond.
- suitable reagents include iminothiolate and methyl-4-mercaptobutyrimidate (1987).
- Abs can be administered in pharmaceutical compositions. Principles and considerations involved in preparing such compositions, as well as guidance in the choice of components can be found in (de Boer, 1994; Gennaro, 2000; Lee, 1990).
- Liposomes can also be used as a delivery vehicle for intracellular introduction. Where antibody fragments are used, the smallest inhibitory fragment that specifically binds to the epitope is preferred.
- peptide molecules can be designed that bind a preferred epitope based on the variable-region sequences of a useful antibody. Such peptides can be synthesized chemically and/or produced by recombinant DNA technology (Marasco et al., 1993).
- Formulations may also contain more than one active compound for a particular treatment, preferably those with activities that do not adversely affect each other.
- the composition can comprise an agent that enhances function, such as a cytotoxic agent, cytokine, chemotherapeutic agent, or growth-inhibitory agent.
- the composition can also contain cells, such as NK-92 cells.
- the active ingredients can also be entrapped in microcapsules prepared by coacervation techniques or by interfacial polymerization; for example, hydroxymethylcellulose or gelatin-microcapsules and poly-(methylmethacrylate) microcapsules, respectively, in colloidal drug delivery systems (for example, liposomes, albumin microspheres, microemulsions, nano-particles, and nanocapsules) or in macroemulsions.
- colloidal drug delivery systems for example, liposomes, albumin microspheres, microemulsions, nano-particles, and nanocapsules
- formulations to be used for in vivo administration are highly preferred to be sterile. This is readily accomplished by filtration through sterile filtration membranes or any of a number of techniques.
- Sustained-release preparations may also be prepared, such as semi-permeable matrices of solid hydrophobic polymers containing the antibody, which matrices are in the form of shaped articles, e.g., films, or microcapsules.
- sustained-release matrices include polyesters, hydrogels (for example, poly(2-hydroxyethyl-methacrylate), or poly(vinylalcohol)), polylactides (Boswell and Scribner, 1973), copolymers of L-glutamic acid and ⁇ ethyl-L-glutamate, non-degradable ethylene-vinyl acetate, degradable lactic acid-glycolic acid copolymers such as injectable microspheres composed of lactic acid-glycolic acid copolymer, and poly-D-(-)-3-hydroxybutyric acid. While polymers such as ethylene-vinyl acetate and lactic acid-glycolic acid enable release of molecules for over 100 days, certain
- the use of multiple antibodies or F(ab')2 fragments to specifically block selected activating receptors permits refinement of the identification of the receptors that are involved in any particular case.
- the presence of NK cell-mediated lysis of a target for which all known activating receptors are blocked is suggestive of the presence of previously unknown activating receptors or ligands.
- the converse experiment of observing the cytolytic activity of native and transduced NK-92 cells against target cells that have been modified so as to express putative ligands for these receptors can provide additional information and possible confirmation.
- the cytokine response of the effector cells in these experiments can also provide additional information. Therefore, the invention offers a myriad of options for refining the assay conditions to suit the user's needs, as well as providing a valuable tool for investigations of basic physiological mechanisms of NK cell function.
- CD16 + effector cells such as native NK cells and the NK-92-CD16 cells and NK-92-CD16 ⁇ / ⁇ cells of this invention bind to the Fc portions of Herceptin or Rituximab antibodies that, in turn, bind via their F(ab) portions to the corresponding cell surface antigen on a cancer cell.
- This ligation of the cancer cell antigen to CD 16 activates the effector cell and directs its cytolytic activity against the cancer cell, thus resulting in its destruction.
- a chimeric "bi-specific antibody” can, by way of example, incorporate one F(ab) binding domain that specifically binds to a cell surface marker that is uniquely or characteristically expressed on the target tumor or infected cells and a second F(ab) domain that specifically engages activating receptors such as CD 16 on NK or other effector cells.
- Such chimeric antibodies are exemplified by the monoclonal antibody 2B1 (Clark et al., 1997; Weiner et al., 1995a; Weiner et al., 1995b) which incorporates one F(ab) domain that specifically binds to the ErbB2 (HER2/neu) antigen and a second F(ab) domain that specifically binds to CD16.
- Cells of the ErbB2 + ovarian cancer line SKOV-3 are only slightly susceptible to cytolysis by NK cells or NK-92-CD16 cells.
- SKOV-3 cells become highly susceptible to NK-92-CD16 cell-mediated cytolysis in the presence of 2B1 antibody which ligates the ErbB2 antigen on a SKOV-3 cell to the CD16 activating receptor on a NK-92-CD16 cell. ( Figure 5 ).
- the effector cell is genetically engineered to express a single polypeptide chain consisting of an antigen-specific monovalent F(ab) binding domain that is covalently linked to a signaling domain, such as TCR- ⁇ (Genbank Accession No. J04132; SEQ ID NO:6).
- ADCC and redirected cytotoxicity assays can be used to identify antibodies and antibody constructs that are useful as therapeutic agents for the treatment of cancers and infections.
- NK-92-CD16, NK-92-CD16- ⁇ or NK-92-CD16- ⁇ cells are used as effector cells in these assays.
- the target cells and the characteristics of the antibody or antibody construct to be evaluated largely determine whether the ADCC or the redirected cytotoxicity assay format is more appropriate.
- a target cell that expresses the ligand of interest, but which does not express any Fc receptors is appropriate for the evaluation of antibodies in the ADCC format. This same type of target cell is also suitable for the ADCC evaluation of antibody constructs that include an Fc domain.
- an antibody construct that incorporates separate F(ab) binding domains that are specific for the antigen of interest and for CD 16 are most appropriately evaluated via redirected cytotoxicity using target cells that express the antigen of interest, but which do not express CD16.
- Other such arrangements are likewise possible and can be used in the practice of the present invention.
- the target cell is typically selected to exhibit NK-92 mediated lysis of between 0% and 30%, preferably between 0% and 20%, more preferably between 0% and 10% and most preferably between 0% and 5%.
- Target cell lines such as SKOV-3 are useful because they exhibit minimal (5%-30%) susceptibility to lysis by NK-92 cells and they constitutively express certain cell surface antigens that are of particular interest as targets for therapeutic antibodies. These cells can also be transduced or transfected to express other antigens of interest and utility.
- One significant application of the present invention is in the screening of hybridoma supernates for the presence of ADCC-inducing monoclonal antibodies.
- the spleen cell fusions employed for the initial generation of monoclonal antibodies result in a heterogeneous population of cells, some of which produce antibodies. Each individual antibody-producing cell in this mixture typically produces a unique antibody that has at least some affinity for the target antigen.
- the cells in this original heterogeneous mixture are sub-cloned, typically by limiting dilution, to the point where each sub-clone originates from a single parent cell. Each sub-clone is then typically screened to eliminate those that do not secrete immunoglobulins.
- the remaining sub-clones which can number in the tens to hundreds, each secrete a unique antibody, a few of which can have specificities, affinities and other characteristics that make them suitable for further evaluation and development as potential therapeutic agents.
- the ADCC and redirected cytotoxicity assays of Example 6 find utility in the screening of clones to identify those sub-clones that secrete potentially useful antibodies of the IgG isotypes. These same assays can subsequently be used to support the evaluation, characterization and further development of these antibodies.
- the present invention consists of NK-92 cell constructs that have been engineered to stably express the fully active, high or low affinity form of the Fc ⁇ RIII (CD16) receptor.
- CD 16 is naturally present on NK cells, but not expressed on parental NK-92 cells and or with any stability by any of the other known NK-like cell lines.
- the transduced NK-92-CD16, NK-92-CD16-y and NK-92-CD16- ⁇ cell lines are, therefore, unique among the presently available NK-like cell lines.
- NK-92 and its genetically engineered derivatives exhibit levels of functional responsiveness in cytotoxicity and cytokine assays that are superior to primary NK cells and most of the other available human NK-like cell lines and appear to be safely tolerated in human subjects.
- the constructs of the present invention when used in combination with an antibody that specifically binds to a cell surface marker that is uniquely or characteristically expressed on the intended target cell, provides a substantially higher level of cytolytic activity and specificity toward the target cell type than is provided by parental NK-92 cells or the antibody alone when used in the same manner.
- the NK-92 constructs of this invention express minimal inhibitory receptors, which makes them reactive toward a broad array of tumors.
- the target cell specificity of these constructs is determined by the co-administered antibody or antibodies, thus permitting these constructs to be used without change for any clinical indication for which a suitable antibody can be prepared.
- Polyclonal antibodies, cocktails consisting of multiple monoclonal antibodies, and chimeric antibody constructs such as bi-specific antibodies, mini-bodies and TriBi (trimeric, bi-specific) antibodies can be beneficially used in conjunction with this invention.
- the present invention can be administered either to animals or to human subjects.
- the most beneficial animal models include RAG-deficient/common ⁇ chain-deficient mice (lacking T, B, and NK cells) or SCID mice (lacking T and B cells); these strains are available from The Jackson Laboratory; Bar Harbor, ME.
- the suppression of the native immune system in such immuno-compromised animals facilitates differentiation between responses induced by the treatment and normal immune responses.
- the cell line derivatives can be used to treat animal subjects, such as bovines, swine, rabbits, alpacas, horses, canines, felines, ferrets, rats, mice, fowl and buffalo, suffering from tumors in combination with tumor-specific antibodies.
- NK-92 cells can be enhanced by preparing subjects who are to receive CD16-transduced NK-92 cells for therapy by infusion the subjects with a low dose of IL-2 for several days prior to administering the NK-92-CD16 cells and targeting antibody, and to continue this infusion for several days afterwards.
- the CD16-transduced NK-92 cells can be prepared from cells of the NK-92mi or NK-92ci cell lines that have been engineered to constitutively express IL-2. In either case, concurrent treatment with IL-2 can increase the survival of the administered NK-92 cells.
- NK-92 cell line Since the NK-92 cell line was isolated from a large granular lymphoma subject, the cells have the potential to establish tumors in recipient subjects. Although this tumorgenicity has not been observed in any subjects (human or animal), accepted practice incorporates ⁇ irradiating NK-92 cells prior to administration at doses levels that suppresses NK-92 cell proliferation while substantially maintaining cytotoxicity and cell survival. Gamma irradiation of NK-92 cells at doses of between about 750 and 1000 Grays, e.g ., 750, 800, 850, 900 and 950 Grays, is considered to be sufficient for this purpose.
- In-vivo treatment of a subject is initiated by administration of the targeting antibody prior to, or concurrently with, the administration of CD 16-transduced NK-92 cells.
- Administration is typically via intravenous or intraperitoneal infusion although direct injection into solid tumors or other such focal lesions can also be used.
- a split-dose regimen can be preferable, particularly when IL-2 is not being co-administered, in order to maintain a high level of active, transduced NK-92 cells in the subject.
- administering the antibody by infusion and the transduced cells by direct injection can be advantageous.
- the efficacy of the treatment is generally assessed by lesion reduction/clearance, cytokine profile or other physiological parameters.
- NK-92-CD16, NK-92-CD16/ ⁇ and NK-92-CD16/ ⁇ cells of the present invention represent stable and reproducible populations of effector cells that are of particular utility in the in-vitro evaluation of antibodies that are being developed as potential therapeutic agents.
- These same cell lines are effective components of in-vivo therapies for the treatment of diseases, including cancers and infections.
- Co-administration of one of these cell lines in conjunction with a antibody that specifically binds to an antigen that is expressed by the tumor or infected cell can potentiate the therapeutic effects of the antibody, thus treating the disease.
- a similar beneficial effect can be observed in such cases where the cell line is administered as a sole therapy to a subject that has developed endogenous antibodies against a tumor or infection.
- Fc receptor CD16 has been exemplified, the present invention is not limited to the expression of FC ⁇ RIII-A, and the expression of other Fc receptors for IgG and other antibody types is also within the scope of the invention, including the classes of Fc ⁇ receptors (e.g ., FC ⁇ RI (CD64), FC ⁇ RII (CD32), FC ⁇ RIII, and FcRn, Fc ⁇ (alpha), Fc ⁇ (epsilon), and their various subclasses. Additional NK-92 variant cell lines also fall within the spirit and scope of this invention.
- FC ⁇ RI CD64
- FC ⁇ RII CD32
- FC ⁇ RIII FC ⁇ RIII
- FcRn Fc ⁇ (alpha), Fc ⁇ (epsilon)
- Additional NK-92 variant cell lines also fall within the spirit and scope of this invention.
- NK-92 can, by way of example, be co-transduced with genes leading to the creation of cell lines such as NK-92ci-CD16 and NK-92mi-CD16 that express both IL-2 and CD16, and that therefore can be used without need for exogenous IL-2.
- NK-92ci-CD16 and NK-92mi-CD16 that express both IL-2 and CD16, and that therefore can be used without need for exogenous IL-2.
- Cells e.g ., modified and unmodified NK-92
- polypeptides and Abs, and derivatives, fragments, analogs and homologs thereof
- Such compositions typically comprise the cell, polypeptide, and/or antibody and a pharmaceutically acceptable carrier.
- a "pharmaceutically acceptable carrier” includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like, compatible with pharmaceutical administration (Gennaro, 2000).
- Preferred examples of such carriers or diluents include, but are not limited to, water, saline, Finger's solutions, dextrose solution, and 5% human serum albumin. Liposomes and non-aqueous vehicles such as fixed oils may also be used. Supplementary active compounds can also be incorporated into the compositions.
- Sterile injectable solutions can be prepared by incorporating the active compound (e.g ., an NK-92 cell and/or antibody) in the required amount in an appropriate solvent with one or a combination of ingredients as required, followed by sterilization.
- the active compound e.g ., an NK-92 cell and/or antibody
- dispersions are prepared by incorporating the active compound into a sterile vehicle that contains a basic dispersion medium, and the other required ingredients as discussed.
- Sterile powders for the preparation of sterile injectable solutions, methods of preparation include vacuum drying and freeze-drying that yield a powder containing the active ingredient and any desired ingredient from a sterile solutions.
- CD 16 cDNA X52645.1 encoding the low affinity form of the transmembrane immunoglobulin ⁇ Fc region receptor III-A (Fc ⁇ RIII-A or CD16) [Phenylalanine-157 (F157), complete sequence: SwissProt P08637 (SEQ ID NO:1)] or a polymorphic variant encoding a higher affinity form of the CD16 receptor [Valine-157 (F157V), complete sequence: SwissProt VAR_008801 (SEQ ID NO:2)] was sub-cloned into the bi-cistronic retroviral expression vector, pBMN-IRES-EGFP (obtained from G. Nolan, Stanford University, Stanford, CA) using the Bam HI and Not I restriction sites in accordance with standard methods.
- pBMN-IRES-EGFP obtained from G. Nolan, Stanford University, Stanford, CA
- the recombinant vector was mixed with 10 ⁇ L of PLUSTM Reagent (Invitrogen; Carlsbad, CA); diluted to 100 ⁇ L with pre-warmed, serum-free Opti-MEM® (Invitrogen; MEM, minimum essential media); further diluted by the addition of 8 ⁇ L LipofectamineTM (Invitrogen) in 100 ⁇ L pre-warmed serum-free Opti-MEM®; and incubated at room temperature for 15 minutes. This mixture was then brought to a total volume of 1 mL by the addition of pre-warmed serum-free Opti-MEM®.
- Phoenix-Amphotropic packaging cells obtained from G.
- FBS fetal bovine serum
- the media was then removed; the cells washed with 6 mL pre-warmed serum-free Opti-MEM®; 2 mL serum-free Opti-MEM® added; and the cells incubated at 37°C, under a 7% CO 2 /balance air atmosphere for an additional 48 hours.
- the virus-containing supernate was collected into a 15 mL plastic centrifuge tube; centrifuged at 1300 rpm for 5 minutes to remove cells and cell fragments; and the supernate transferred to another 15 mL plastic centrifuge tube.
- 20 ⁇ L of PLUSTM Reagent was added to the virus suspension; the mixture incubated at room temperature for 15 minutes; 8 ⁇ L LipofectamineTM added to the mixture; and the mixture incubated for an additional 15 minutes at room temperature.
- NK-92 cells cultured in ⁇ -MEM (Sigma; St. Louis, MO) supplemented with 12.5% FBS, 12.5% fetal horse serum (FHS) and 500 IU rhIL-2/ mL (Chiron; Emeryville, CA) were collected by centrifugation at 1300 rpm for 5 minutes, and the cell pellet was re-suspended in 10 mL serum-free Opti-MEM® medium. An aliquot of cell suspension containing 5 x 10 4 cells was sedimented at 1300 rpm for 5 minutes; the cell pellet re-suspended in 2 mL of the retrovirus suspension described in Example 1, and the cells plated into 12-well culture plates.
- the plates were centrifuged at 1800 rpm for 30 minutes and incubated at 37°C under an atmosphere of 7% CO 2 /balance air for 3 hours. This cycle of centrifugation and incubation was then repeated a second time.
- the cells were diluted with 8 mL of ⁇ -MEM, transferred to a T-25 flask, and incubated at 37°C under a 7% CO 2 /balance air until the cells were confluent.
- the transduced cells were collected, re-suspended in serum-free Opti-MEM® medium, and sorted on the basis of their level of EGFP expression using a fluorescence activated cell sorter (FACS), EGFP being co-expressed with, and a surrogate marker for, CD16.
- FACS fluorescence activated cell sorter
- CD16 Cell-surface expression of CD16 was confirmed by immuno-staining the transduced cells with an anti-CD16 antibody.
- the transduced cells which are designated as NK-92-CD16, were passed with fresh IL-2 every 4 days and assayed for cell-surface expression of CD16 before use.
- Figures 1A and 1B are flow cytometer scatter diagrams showing NK-92 cells transduced with CD16 cDNA using the pBMN-IRES-EGFP vector after staining with secondary phycoerythrin (PE)-conjugated anti-mouse IgG antibody alone ( Figure 1A ) or anti-CD16 antibody (3G8 (Fleit et al ., 1982; Perussia and Trinchieri, 1984); mouse IgG) + PE-anti-mouse IgG ( Figure 1B ) and analysis using a FACS (Becton Dickinson; Franklin Lakes, NJ) flow cytometer. EGFP expression is assessed on the x-axis and surface CD16 expression is on the y-axis.
- Figure 1 illustrates that the NK-92-CD16 cell line expresses CD16 on the cell surface when stained with a monoclonal anti-CD16 antibody.
- Example 3 NK-92-CD16 cells co-expressing CD16 and an accessory signaling protein Fc ⁇ RI- ⁇ or TCR- ⁇
- Recombinant retroviruses incorporating inserted genes for the expression of either accessory signaling proteins, Fc ⁇ RI- ⁇ (SEQ ID NO:5) or TCR- ⁇ (SEQ ID NO:7) were prepared by using standard methods to ligate the corresponding cDNA into the pBMN-IRES-EGFP vector and transfecting this construct into the Phoenix-Amphotropic packaging cell line in the presence of LipofectamineTM Plus as described in Example 1.
- the resulting ⁇ or ⁇ recombinant retroviruses were used to transduce NK-92 cells as described in Example 2 with the following further modifications.
- NK-92 cells transduced with Fc ⁇ RI- ⁇ polynucleotide (SEQ ID NO:4) or TCR- ⁇ (SEQ ID NO:6) were collected, re-suspended in serum-free Opti-MEM® medium and sorted on the basis of their level of the co-expressed EGFP using a FACS, CD16 cDNA was ligated into a version of the pBMN vector lacking the IRES and EGFP sequences, called pBMN-NoGFP (Yusa et al ., 2002).
- the ⁇ - or ⁇ -transduced NK-92 cells were secondarily co-transduced with CD16-pBMN-NoGFP using the same retroviral transduction method as described in Example 2.
- the co-transduced cells were suspended in ⁇ -MEM, transferred to a T-25 flask, and grown to confluency at 37°C under a 7% CO 2 /balance air. After reaching confluency, the co-transduced cells were immuno-stained with an anti-CD 16 antibody and sorted by FACS for cell-surface expression of CD 16. The selected cells were sub-cultured with fresh IL-2 every four days and assayed for cell-surface expression of CD 16 before use.
- EGFP fluorescence is a surrogate indicator for the level of expression of the accessory signaling protein.
- An anti-CD16 antibody conjugated to a fluorophore having an emission spectrum different from that of EGFP was employed to determine the level of expression of CD 16.
- Figure 2 shows flow cytometer scatter diagrams showing the expression of CD 16 by NK-92 cells transduced with CD16 alone ( Figure 2A ) and the increase in CD 16 expression when NK-92 cells are transduced with CD16 cDNA in combination with Fc ⁇ RI- ⁇ cDNA ( ⁇ ; Figure 2B ); or CD3 ⁇ cDNA ( ⁇ , Figure 2C).
- Figure 2 shows that when CD 16 is co-expressed with Fc ⁇ RI- ⁇ or CD3 ⁇ in the NK-92 cell line, the cell-surface expression of CD16 is increased over that obtained when NK-92 cells are transduced with CD 16 alone.
- the transduced NK-92 cells used in these assays were generally selected for maximal CD16 expression as previously described.
- Raji cells e.g., ATCC Deposit No. CCL-86
- NK-92 cells e.g., ATCC Deposit No. CCL-86
- Approximately 2x10 6 of the selected target cells were washed by suspension in RPMI medium and sedimentation at 1300 rpm for 5 minutes. After removal of the supernate, 20 ⁇ L of FBS and 100 ⁇ Ci of Na[ 51 Cr]chromate was added and the cells incubated at 37° C for 60-90 minutes with mixing every 30 minutes. The labeled target cells were washed three times by suspension in 10 mL of RPMI medium and sedimentation at 1500 rpm for 5 minutes. The final cell pellet was re-suspended in ⁇ -MEM and diluted to a concentration of 1x10 5 /mL. Target cells for use in redirected cytotoxicity or ADCC assays were further incubated with the appropriate antibody at a final concentration of 0.01-5 ⁇ g/mL for 10-15 minutes at room temperature.
- One-hundered ⁇ L of the selected type of target cells and 100 ⁇ L of the appropriate concentration of effector cells were added to each well of a 96 well V-bottom plate. Three to six replicate wells were prepared at each E:T ratio. At least 6 wells were allocated to each of a spontaneous lysis control (effector cells replaced with 100 ⁇ L of ⁇ -MEM) and total release control (effector cells replaced with 100 ⁇ L of 2% t-Octylphenoxypolyethoxyethanol (Triton X-100®)detergent in ⁇ -MEM). Desirably, an additional six or more wells are allocated to the use of unmodified NK-92 effector cells that do not express CD16 as a procedural control and internal standard.
- the plate was then centrifuged at 500 rpm for 3 minutes and incubated for 4 hours at 37° C in an atmosphere of 7% CO 2 /balance air. At the end of the incubation period, the plate was centrifuged at 1500 rpm for 8 minutes, and 100 ⁇ L of the supernate was collected from each well for counting in a ⁇ counter to measure of 51 Cr release.
- a monoclonal antibody specific for CD16 was used in redirected cytotoxicity assays in those cases where a target cell line that expressed a Fc receptor other than CD16 was available.
- the FcgR+ mouse mastocytoma cell line P815 and human Fc ⁇ R + myelocytic cell line THP-1 were used as targets in combination with the anti-CD 16 monoclonal antibody (mAb) 3G8 (Fleit et al ., 1982; Perussia and Trinchieri, 1984) to evaluate NK-92-CD16, NK-92-CD16- ⁇ and NK-92-CD16- ⁇ cells ( Figures 3 and 4 ).
- the target cell receptor is thought to bind the Fc portion of the antibody, while the F(ab) portion of the antibody binds to CD 16 on the effector cell.
- redirected cytotoxicity assays can be performed using target cells that express a unique antigen, but which do not express a Fc receptor, in conjunction with a bi-specific antibody construct.
- one F(ab) binding domain of the bi-specific antibody specifically binds the target cell antigen while another F(ab) domain specifically binds to CD16.
- NK-92-CD16, NK-92-CD16- ⁇ or NK-92-CD16- ⁇ cells in this format was carried out using SKOV-3 as target cells and the chimeric antibody 2B1 as the cross-linking agent.
- the 2B1 chimeric bi-specific antibody has one binding domain that is specific for HER2/neu and a second binding domain that is specific for CD16 (Clark et al ., 1997; Weiner et al ., 1995a; Weiner et al ., 1995b) ( Figure 5 ).
- Figure 6 illustrates the cytotoxicity of NK-92-CD16, NK-92-CD16- ⁇ and NK-92-CD16- ⁇ cells against P815 target cells in a redirected cytotoxicity assay using 2B1 chimeric antibody after pefroming a 51 Cr-release assay for four hours.
- This Figure shows that at less than saturating antibody concentrations, cytotoxicity is a function of both antibody concentration and the level of expression of CD16 on the NK-92 effector cells.
- the following procedure was used in performing both ADCC and redirected cytotoxicity assays, the type of assay being determined by the characteristics of the target cell and selected antibody.
- the selected target cells were labeled with Na[ 51 Cr]chromate as described in Example 4. Aliquots of the 51 [Cr]-labeled target cells were further incubated with the selected antibody at multiple concentrations between 0.01 ⁇ g and 5 ⁇ g/mL for 15 minutes at room temperature, washed with ⁇ -MEM, and adjusted to a concentration of 1x10 5 cells/mL before use.
- At least 6 wells were allocated to each of a spontaneous lysis control (effector cells replaced with 100 ⁇ L of ⁇ -MEM) and total release control (effector cells replaced with 100 ⁇ L of 2% Triton X-100 detergent in ⁇ -MEM).
- An additional three wells at each E:T ratio were allocated to "non-ADCC" controls in which the target cells were not exposed to the antibody.
- an additional 6 or more wells are allocated to the use of unmodified NK-92 effector cells that do not express CD16 as a procedural control and internal standard.
- the plate was then centrifuged at 500 rpm for 3 minutes and incubated for 4 hours at 37° C in an atmosphere of 7% CO 2 /balance air.
- the plate was centrifuged at 1500 rpm for 8 minutes and 100 mL of the supernate was collected from each well for counting in a ⁇ counter as a measure of 51 [Cr] release due to cytotoxicity.
- the percentage of specific lysis was calculated as described in Example 4.
- NK-92-CD16 cells expressing varying surface levels of CD16 (through cell sorting or via ⁇ or ⁇ co-transduction), as well as NK-92 transduced with the high affinity polymorphic allele of the CD16 gene (F157V).
- F157V high affinity polymorphic allele of the CD16 gene
- the selected target cells were labeled with Na[ 51 Cr]chromate as described in Example 4 and adjusted to a concentration of 1x10 5 cells/mL before use. A 100 ⁇ L aliquot of labeled target cells was then transferred to each well of the requisite number of 96-well plates.
- the immunoglobulin concentrations in the hybridoma supernates to be screened were optionally, but preferably, adjusted to a convenient nominal concentration of 1 ⁇ g/mL. At least 100 ⁇ L aliquots of each hybridoma supernate was added to each of three target cell containing wells; incubated for 15 minutes at room temperature, washed with ⁇ -MEM, and re-suspended in 100 ⁇ L of ⁇ -MEM.
- the effector cell concentration was adjusted as appropriate to achieve the desired E:T ratio in the assay. For example, if an E:T ratio of 10:1 was desired, the effector cell concentration was adjusted to 1x10 6 cells/mL.
- the assay was initiated by adding 100 ⁇ L of effector cells to each well. The plates were then centrifuged at 500 RPM for 3 minutes and incubated for 4 hours at 37° C in an atmosphere of 7% CO 2 /balance air. At the end of the incubation period, the plate was centrifuged at 1500 rpm for 8 minutes and 100 ⁇ L of the supernate was collected from each well for counting in a ⁇ counter as a measure of 51 [Cr] release due to cytotoxicity. The percentage of specific lysis was calculated as described in Example 4.
- At least six wells were allocated to each of a spontaneous lysis control (effector cells replaced with 100 ⁇ L of ⁇ -MEM) and a total release control (effector cells replaced with 100 ⁇ L of 2% Triton X-100 detergent in ⁇ -MEM) on each plate.
- An additional six wells in each set of plates was allocated to each of a "no antibody" control (target cells not treated with antibody) and a NK-92 cytolysis control. Specific lysis was reported as the average of three replicate wells after correction for the appropriate controls.
- Efficacy can be likewise be assessed by the measurement of surrogate indicators such as cytokine release by the NK-92-CD16 cells, the up-regulation of NK cell activation markers such as CD25, CD69 and/or CD95L, activation of transcription factors, such as NF-AT or NF- ⁇ B within the NK-92 cells, or the activation of caspases or other markers of apoptosis in the target cells.
- surrogate indicators such as cytokine release by the NK-92-CD16 cells, the up-regulation of NK cell activation markers such as CD25, CD69 and/or CD95L, activation of transcription factors, such as NF-AT or NF- ⁇ B within the NK-92 cells, or the activation of caspases or other markers of apoptosis in the target cells.
- Example 7 CD16 mediated cytokine production.
- NK-92 cells Upon activation, NK-92 cells are known to produce and secrete cytokines, including interferon- ⁇ (IFN- ⁇ ), tumor necrosis factor (TNF- ⁇ and others), interleukins (IL)-5, -10 and-13, granulocyte-macrophage colony-stimulating factor (GM-CSF), nitric oxide and others upon activation.
- IFN- ⁇ interferon- ⁇
- TNF- ⁇ and others tumor necrosis factor
- IL-5, -10 and-13 interleukins
- GM-CSF granulocyte-macrophage colony-stimulating factor
- nitric oxide nitric oxide and others upon activation.
- the production of these cytokines can be determined by standard methods including cytokine-specific enzyme-linked immunosorbant assay (ELISA) kits that are available from multiple commercial sources (e.g., BD Phramingen; San Diego, CA).
- ELISA cytokine-specific enzyme-
- cytokines by NK-92, NK-92-CD16, NK-92-CD16- ⁇ and NK-92-CD16- ⁇ cells in response to CD16 mediated stimulation can be determined in a manner that is analogous to the ADCC and redirected cytotoxicity assays described in Examples 4 and 5.
- Effector cells were washed by suspension in ⁇ -MEM (without IL-2) and sedimentation at 1300 rpm for 5 minutes.
- the type of target cell used in these assays was selected on the basis of the requirements of the particular determination being performed.
- Raji cells which are known to be moderately susceptible (about 50% lysis under these conditions) to lysis by NK-92 cells, were used for most purposes, including verification of the cytotoxicity of the effector cells.
- One hundred ⁇ L of varying concentrations of effector cells were combined with a constant concentration of antibody treated target cells (not labeled with 51 [Cr]) in wells of a 96-well V-bottom plate. Three to six replicate wells were prepared at each E:T ratio to be evaluated. At least 6 wells each were allocated as controls for non-CD 16 specific effector cell activation in which the target cells were replaced with 100 mL of ⁇ -MEM (spontaneous release) or with 100 ⁇ L of 2% Triton X-100 (total release). Additional controls using target cells that have not been antibody treated and target or effector cells that had been treated with F(ab') 2 fragments to suppress non-CD16 specific effector cell activation were also included as appropriate.
- Transduced NK-92 cells expressing different levels or affinities of CD16 could have been used as additional controls in the manner previously described.
- the plate was centrifuged at 500 rpm for 3 minutes and incubated for 4 hours at 37° C in an atmosphere of 7% CO 2 /balance air. At the end of the incubation period, the plate was centrifuged at 1500 rpm for 8 minutes, and aliquots of the supernate were collected from each well to quantify cytokine concentrations, using commercially available cytokine ELISA kits (e.g., BD Phramingen; San Diego, CA). Effector cell cytokine production was generally determined to track effector cell cytotoxicity and could therefore be taken as an alternative indicator of effector cell activation.
- Example 8 NK-92 cell stimulation by IL-2
- cytokines particularly IL-2, IL-12, IL-15 and IL-18, are known to promote the growth, survival, cytotoxicity and cytokine releasing activities of NK, NK-92, NK-92-CD16, NK-92-CD16- ⁇ and NK-92-CD16- ⁇ , and other NK-92 variant cells both in-vitro and in-vivo.
- the cells transduced in Examples 2 and 3 proliferated and exhibited stable levels of CD 16 expression, cytotoxicity and cytokine response for several months without the need for antibiotic selection when sub-cultured with fresh IL-2-containing medium every 4 days.
- the NK-92mi or NK-92ci cell line that has been engineered to express endogenous IL-2 at levels that promote NK-92 proliferation, survival and activity can also be employed.
- the NK-92mi, NK-92ci and other NK-92 derived cell lines can be transduced in the same manners as described for the parent NK-92 cell line in Examples 2 and 3.
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